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The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease

Improvements have been made in the diagnosis of Alzheimer’s disease (AD), manifesting mostly in the development of in vivo imaging methods that allow for the detection of pathological changes in AD by magnetic resonance imaging (MRI) and positron emission tomography (PET) scans. Many of these imagin...

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Autores principales: Viola, Kirsten L., Bicca, Maira A., Bebenek, Adrian M., Kranz, Daniel L., Nandwana, Vikas, Waters, Emily A., Haney, Chad R., Lee, Maxwell, Gupta, Abhay, Brahmbhatt, Zachary, Huang, Weijian, Chang, Ting-Tung, Peck, Anderson, Valdez, Clarissa, Dravid, Vinayak P., Klein, William L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761808/
https://www.ncbi.nlm.nih.gov/pubmed/35046767
http://dx.doi.org/10.3389/fnins.2021.768646
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author Viola, Kirsten L.
Bicca, Maira A.
Bebenek, Adrian M.
Kranz, Daniel L.
Nandwana, Vikas
Waters, Emily A.
Haney, Chad R.
Lee, Maxwell
Gupta, Abhay
Brahmbhatt, Zachary
Huang, Weijian
Chang, Ting-Tung
Peck, Anderson
Valdez, Clarissa
Dravid, Vinayak P.
Klein, William L.
author_facet Viola, Kirsten L.
Bicca, Maira A.
Bebenek, Adrian M.
Kranz, Daniel L.
Nandwana, Vikas
Waters, Emily A.
Haney, Chad R.
Lee, Maxwell
Gupta, Abhay
Brahmbhatt, Zachary
Huang, Weijian
Chang, Ting-Tung
Peck, Anderson
Valdez, Clarissa
Dravid, Vinayak P.
Klein, William L.
author_sort Viola, Kirsten L.
collection PubMed
description Improvements have been made in the diagnosis of Alzheimer’s disease (AD), manifesting mostly in the development of in vivo imaging methods that allow for the detection of pathological changes in AD by magnetic resonance imaging (MRI) and positron emission tomography (PET) scans. Many of these imaging methods, however, use agents that probe amyloid fibrils and plaques–species that do not correlate well with disease progression and are not present at the earliest stages of the disease. Amyloid β oligomers (AβOs), rather, are now widely accepted as the Aβ species most germane to AD onset and progression. Here we report evidence further supporting the role of AβOs as pathological instigators of AD and introduce promising anti-AβO diagnostic probes capable of distinguishing the 5xFAD mouse model from wild type mice by PET and MRI. In a developmental study, Aβ oligomers in 5xFAD mice were found to appear at 3 months of age, just prior to the onset of memory dysfunction, and spread as memory worsened. The increase of AβOs is prominent in the subiculum and correlates with concomitant development of reactive astrocytosis. The impact of these AβOs on memory is in harmony with findings that intraventricular injection of synthetic AβOs into wild type mice induced hippocampal dependent memory dysfunction within 24 h. Compelling support for the conclusion that endogenous AβOs cause memory loss was found in experiments showing that intranasal inoculation of AβO-selective antibodies into 5xFAD mice completely restored memory function, measured 30–40 days post-inoculation. These antibodies, which were modified to give MRI and PET imaging probes, were able to distinguish 5xFAD mice from wild type littermates. These results provide strong support for the role of AβOs in instigating memory loss and salient AD neuropathology, and they demonstrate that AβO selective antibodies have potential both for therapeutics and for diagnostics.
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spelling pubmed-87618082022-01-18 The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease Viola, Kirsten L. Bicca, Maira A. Bebenek, Adrian M. Kranz, Daniel L. Nandwana, Vikas Waters, Emily A. Haney, Chad R. Lee, Maxwell Gupta, Abhay Brahmbhatt, Zachary Huang, Weijian Chang, Ting-Tung Peck, Anderson Valdez, Clarissa Dravid, Vinayak P. Klein, William L. Front Neurosci Neuroscience Improvements have been made in the diagnosis of Alzheimer’s disease (AD), manifesting mostly in the development of in vivo imaging methods that allow for the detection of pathological changes in AD by magnetic resonance imaging (MRI) and positron emission tomography (PET) scans. Many of these imaging methods, however, use agents that probe amyloid fibrils and plaques–species that do not correlate well with disease progression and are not present at the earliest stages of the disease. Amyloid β oligomers (AβOs), rather, are now widely accepted as the Aβ species most germane to AD onset and progression. Here we report evidence further supporting the role of AβOs as pathological instigators of AD and introduce promising anti-AβO diagnostic probes capable of distinguishing the 5xFAD mouse model from wild type mice by PET and MRI. In a developmental study, Aβ oligomers in 5xFAD mice were found to appear at 3 months of age, just prior to the onset of memory dysfunction, and spread as memory worsened. The increase of AβOs is prominent in the subiculum and correlates with concomitant development of reactive astrocytosis. The impact of these AβOs on memory is in harmony with findings that intraventricular injection of synthetic AβOs into wild type mice induced hippocampal dependent memory dysfunction within 24 h. Compelling support for the conclusion that endogenous AβOs cause memory loss was found in experiments showing that intranasal inoculation of AβO-selective antibodies into 5xFAD mice completely restored memory function, measured 30–40 days post-inoculation. These antibodies, which were modified to give MRI and PET imaging probes, were able to distinguish 5xFAD mice from wild type littermates. These results provide strong support for the role of AβOs in instigating memory loss and salient AD neuropathology, and they demonstrate that AβO selective antibodies have potential both for therapeutics and for diagnostics. Frontiers Media S.A. 2022-01-03 /pmc/articles/PMC8761808/ /pubmed/35046767 http://dx.doi.org/10.3389/fnins.2021.768646 Text en Copyright © 2022 Viola, Bicca, Bebenek, Kranz, Nandwana, Waters, Haney, Lee, Gupta, Brahmbhatt, Huang, Chang, Peck, Valdez, Dravid and Klein. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Viola, Kirsten L.
Bicca, Maira A.
Bebenek, Adrian M.
Kranz, Daniel L.
Nandwana, Vikas
Waters, Emily A.
Haney, Chad R.
Lee, Maxwell
Gupta, Abhay
Brahmbhatt, Zachary
Huang, Weijian
Chang, Ting-Tung
Peck, Anderson
Valdez, Clarissa
Dravid, Vinayak P.
Klein, William L.
The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease
title The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease
title_full The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease
title_fullStr The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease
title_full_unstemmed The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease
title_short The Therapeutic and Diagnostic Potential of Amyloid β Oligomers Selective Antibodies to Treat Alzheimer’s Disease
title_sort therapeutic and diagnostic potential of amyloid β oligomers selective antibodies to treat alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761808/
https://www.ncbi.nlm.nih.gov/pubmed/35046767
http://dx.doi.org/10.3389/fnins.2021.768646
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